Label: HEAD AND SHOULDERS SUPREME DETOX AND HYDRATE CONDITIONER- pyrithione zinc lotion

  • NDC Code(s): 69423-347-27
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 27, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Pyrithione zinc 0.5%

  • Purpose

    Anti-dandruff

  • Uses

    helps prevent recurrence of flaking and itching associated with dandruff.

  • Warnings

    For external use only.

    When using this product

    • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    • condition worsens or does not improve after regular use of this product as directed.

    Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • for best results use at least twice a week or as directed by a doctor.
    • apply to wet hair after shampooing by gently massaging into hair and scalp, rinse well.
  • Inactive ingredients

    Water, stearyl alcohol, behentrimonium chloride, cetyl alcohol, argania spinosa kernel oil, zea mays (corn) silk extract, cocos nucifera (coconut) fruit extract, fragrance, phenoxyethanol, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone

  • Questions (or comments)?

    1-800-723-9569

  • SPL UNCLASSIFIED SECTION

    Dist. by PROCTER & GAMBLE,
    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 247 mL Tube Label

    head &
    shoulders ®
    PYRITHION ZINC DANDRUFF

    SCALP & HAIR CONDITIONER

    SUPREME

    DETOX &

    HYDRATE

    WITH ARGAN OIL & COCONUT WATER

    FREE FROM

    SULFATES

    PARABENS

    PHTHALATES

    DYES

    9.4 FL OZ
    (278 mL)

    HS

  • INGREDIENTS AND APPEARANCE
    HEAD AND SHOULDERS SUPREME DETOX AND HYDRATE CONDITIONER 
    pyrithione zinc lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-347
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    CORN SILK (UNII: 7D3VB244UX)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    WATER (UNII: 059QF0KO0R)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-347-27278 mL in 1 TUBE; Type 0: Not a Combination Product05/02/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03205/02/2019
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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